ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA— 510(k) K884962

Name: FDA 510(k) clearance K884962
Creator: U.S. Food and Drug Administration
Published: 1990-02-09

Substantially Equivalent

Bausch & Lomb Pharmaceutical, Inc.

FDA 510(k) clearance K884962 for ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA, Substantially Equivalent on 1990-02-09. Applicant: Bausch & Lomb Pharmaceutical, Inc.. Device class: 1.

Clearance details

Applicant: Bausch & Lomb Pharmaceutical, Inc.
Product code: Code MOE
Device class: Class 1
Regulation: 21 CFR 886.4750
Advisory panel: Ophthalmic
Date received: 1988-11-18
Decision date: 1990-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

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